HRID915949
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a 10 ml toluene solution of 160 mg (0.35 mmol) of the compound obtained in Example 122, 135 mg (0.71 mmol) of p-toluenesulfonic acid monohydrate was added, and the mixture was heated under reflux for 22 hours with the use of a Dean-Stark dehydrator. The reaction mixture was returned to room temperature, and washed with a saturated aqueous solution of sodium hydrogen carbonate. The system was dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=30/1) to obtain 78 mg (51%) of the captioned compound.
WORKUP
后处理
- temperaturethe mixture was heated
- temperatureunder reflux for 22 hours with the use of a Dean-Stark dehydrator
- customwas returned to room temperature
- washwashed with a saturated aqueous solution of sodium hydrogen carbonate
- dry with materialThe system was dried over anhydrous sodium sulfate
- distillationthe solvent was distilled off under reduced pressure
- customThe residue was purified by silica gel column chromatography (chloroform/methanol=30/1)